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Merck

SCP0058

Sigma-Aldrich

Bradykinin Peptide

≥95% (HPLC), lyophilized powder

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About This Item

Empirische Formel (Hill-System):
C59H89N17O14
Molekulargewicht:
1260.44
UNSPSC-Code:
12352202
NACRES:
NA.32

product name

Bradykinin Ile-Ser, T-Kinin,

Assay

≥95% (HPLC)

Form

lyophilized

Zusammensetzung

Peptide Content, ≥65%

Lagerbedingungen

protect from light

Lagertemp.

−20°C

Amino Acid Sequence

Ile-Ser-Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg

Anwendung

Bradykinin, a nonapeptide, is a potent endothelium-dependent vasodilator that operates via bradykinin receptors B1 and B2. Bradykinin Ile-Ser (T-Kinin) has a biological profile similar but not identical to bradykinin which is more resistant to degradation by kininase angiotensin converting enzyme (ACE). Bradykinin Ile-Ser is used to differentiate bradykinin receptor specificity and function.

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Die Dokumentenbibliothek aufrufen

Prashant Desai et al.
European journal of medicinal chemistry, 37(2), 135-146 (2002-02-23)
T-kinin (Ile-Ser-BK) is related to BK in its biological profile, but unlike BK, is more resistant to the action of ACE. A detailed NMR and molecular modeling study of T-kinin has been carried out in three diverse media: water (pH
Clare Davis et al.
European journal of pharmacology, 450(2), 123-130 (2002-09-11)
T-kinin and its putative carboxypeptidase product des-Arg(11)-T-kinin are members of the kinin family that are unique to the rat. Primary cultures of rat bladder smooth muscle cells were used to investigate the pharmacology of these peptides. Calcium imaging experiments showed
D G Sawutz et al.
European journal of pharmacology, 227(3), 309-315 (1992-11-02)
[3H]Bradykinin binds to intact human IMR-90 fetal lung fibroblasts in a time and dose-dependent manner. Binding equilibrium was attained by 120 minutes at 4 degrees C. [3H]Bradykinin binding was saturable; Scatchard analysis of saturation binding data demonstrated a single binding
Anna Bernhold Brechter et al.
Regulatory peptides, 103(1), 39-51 (2001-12-12)
Bradykinin receptor subtypes linked to prostaglandin release have been assessed in a human osteosarcoma cell line with osteoblastic phenotype (MG-63). Bradykinin (BK; 1 micromol/l) caused a burst of prostaglandin E(2) release that was maximal at 10 min. When the effect

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